Deposition of Submicron Particles by Chaotic Mixing in the Pulmonary Acinus: Acinar Chaotic Mixing

Deposition of Submicron Particles by Chaotic Mixing in the Pulmonary Acinus: Acinar Chaotic Mixing

Akira Tsuda, Frank S. Henry
DOI: 10.4018/978-1-7998-7156-9.ch011
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Abstract

In this review, the authors outline the evidence that emerged some 30 years ago that the mechanisms thought responsible for the deposition of submicron particles in the respiratory region of the lung were inadequate to explain the measured rate of deposition. They then discuss the background and theory of what is believed to be the missing mechanism, namely chaotic mixing. Specifically, they outline how that the recirculating flow in the alveoli has a range of frequencies of oscillation and some of these resonate with the breathing frequency. If the system is perturbed, the resonating frequencies break into chaos, and they discuss a number of practical ways in which the system can be disturbed. The perturbation of fluid particle trajectories results in Hamiltonian chaos, which produces qualitative changes in those trajectories. They end the review with a discussion of the effects of chaotic mixing on the deposition of inhaled particles in the respiratory region of the lung.
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Introduction

The primary purpose of the lung is gas exchange. Oxygen-rich air is drawn into the lung by the diaphragm and intercostal muscles, and carbon dioxide and other gasses are rejected with the outgoing air when the muscles relax. This rhythmic, in-and-out, motion of the lungs happens twelve times a minute on average (Weibel, 1984).

The anatomy of the lung may be divided into three regions: upper airways (nasal pharynx area), conducting airways (trachea to terminal bronchioles) and the pulmonary acinus (respiratory bronchioles to terminal alveolar ducts). Each region has its own unique anatomy and flow regime (West, 2012). Despite these differences in anatomy and flow type, particles are carried from the mouth to the lung periphery.

For a particle to deposit on the surface of the alveolar blood-air barrier, two things have to occur. First, the particle has to travel with the ambient air through a network of ducts and end up close to the alveolar surface. Second, if the particle is close enough, short-distance forces acting on the particle (e.g., the van der Waals force, electrostatic force, Brownian force, etc. [Friedlander, 1977]) will be sufficient to bring it to the surface.

In the lung physiology literature (e.g., West, 2012; Oberdörster et al. 2007), three mechanisms are typically defined as contributing to particle deposition. These are inertial impaction, gravitational sedimentation, and Brownian motion.

Inertial impaction: describes the situation in which a particle with relatively large mass (typically a relatively large particle, since mass is proportional to the cube of the particle’s diameter) cannot follow the curvilinear airflow patterns faithfully; and as a result, it deviates from the airflow streamlines and the particle’s own inertia carries it to the surface (Friedlander, 1977). This phenomenon is significant when airflow velocity (978-1-7998-7156-9.ch011.m01) is large, and thus it occurs predominantly in the upper/large airways. A particle’s inertia is consider significant when the Stokes number, 978-1-7998-7156-9.ch011.m02. The Stokes number, 978-1-7998-7156-9.ch011.m03, where 978-1-7998-7156-9.ch011.m04 is the particle density, 978-1-7998-7156-9.ch011.m05 is the particle diameter, 978-1-7998-7156-9.ch011.m06 is the air viscosity, and 978-1-7998-7156-9.ch011.m07 is the characteristic length scale.

Sedimentation: particles with large mass are also subject to the external gravitational force, which makes the particles deposit in the direction of gravity (Tsuda et al. 2013). This phenomenon becomes significant when the particle sedimentation velocity (expressed in terms of the terminal velocity 978-1-7998-7156-9.ch011.m08, where g = gravitational acceleration) becomes comparable to, or more than, the airflow velocity. Deposition by sedimentation occurs primarily in the large airways and at the beginning of the acinus.

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